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Project Manager Late-Stage Production
1 week ago
- Master's degree in relevant natural sciences.
- 8+ years of experience in biopharmaceutical, preferably with therapeutic monoclonal antibody or ADCs.
- 8+ years of experience in CMC project management.
- Proven track record and technical skills in biological process development/biopharmaceutical manufacturing.
- As Genmab primarily uses Contract Manufacturing Organizations (CMOs) for development and GMP manufacture, experience in running projects with external partners is preferred.
- Experience with the CMC technical sections of regulatory submissions and interacting with global regulatory authorities.
- Excellent communication skills in English and the ability to work in multicultural teams.
- Ability to work successfully under pressure in a fast-paced environment and with tight timelines.
- You are passionate about our purpose and genuinely care about our mission to transform the lives of patients through innovative cancer treatment.
- You bring rigor and excellence to all that you do.
- You are a fierce believer in our rooted-in-science approach to problem-solving.
- You are a generous collaborator who can work in teams with diverse backgrounds.
- You are determined to do and be your best and take pride in enabling the best work of others on the team.
- You are not afraid to grapple with the unknown and be innovative.
- You have experience working in a fast-growing, dynamic company (or a strong desire to).
- You work hard and are not afraid to have a little fun while you do so.
